Canonical Allele Identifier: PA2827010774
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1519233
ClinVar RCV Id: RCV002024455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Tyr1434His
CA394304973
NM_001318829.2:c.4300T>C